Organic Chemistry II
	Professor Carl C. Wamser
Chem 335 - Winter 2006	Exam 2

1. (15 points) Write accurate structures for each of the following.

a) isobutyl magnesium bromide

b) lithium dibenzylcuprate

c) any vicinal diol

d) diphenyl disulfide

e) trans-2-methylthiocyclopentanethiol

2. (15 points) Show clear electron-pushing arrows that illustrate how the following compounds are converted into the indicated products. WRITE ONLY ARROWS ON THIS PAGE.

a)

b)

c)

d)

e)

3. (15 points) Complete the following reactions by adding the missing part: either the final product or the necessary reagents and conditions.

a)

b)

c)

d)

e)

4. (20 points) Give clear explanations for the following:

a) (5 points) How can meta- and para-xylene (dimethylbenzene) be distinguished solely by C-13 NMR?

b) (5 points) What would be expected for the parent molecular ion peaks of CH2Br2 , assuming that the natural abundance of Br is equally Br-79 and Br-81? (Indicate expected m/z values with relative intensities.)

c) (10 points) How can each of the following isomers of C3H6O be distinguished solely by IR?

5. (20 points) Show reaction sequences that could be used to efficiently prepare the following two compounds. You must start with alcohols having four carbons or fewer.

6. (15 points) Identify the unknown compound that is formed by reaction of phenyllithium with ethylene oxide and gives the spectral data below. Indicate what can be concluded from each piece of data, and assign the C-13 and H-1 NMR absorptions to specific carbons and hydrogens in your final structure.

IR: strong, broad peak at 3400 cm-1

MS: parent molecular ion at m/z = 122

C-13 NMR: peaks at 40, 60, 115, 120, 125, 140 ppm

H-1 NMR:
a 2.0 ppm, 1H, broad singlet
b 2.7 ppm, 2H, triplet
c 3.6 ppm, 2H, triplet
d 7.0 ppm, 5H, broad multiplet